COVID-19 and One-Carbon Metabolism

被引:13
|
作者
Perla-Kajan, Joanna [1 ]
Jakubowski, Hieronim [1 ,2 ]
机构
[1] Univ Life Sci, Dept Biochem & Biotechnol, PL-60632 Poznan, Poland
[2] Rutgers New Jersey Med Sch, Dept Microbiol Biochem & Mol Genet, Newark, NJ 07103 USA
基金
美国国家科学基金会;
关键词
folate; purine biosynthesis; methionine; S-adenosylmethionine; S-adenosylhomocysteine; homocysteine; cysteine; glutathione; choline; methionine sulfoxide; POTENTIAL PREDICTOR; CARDIOVASCULAR RISK; CONVERTING ENZYME; SPIKE PROTEIN; SARS-COV; DISEASE; ACE2; HOMOCYSTEINE; SARS-COV-2; RECEPTOR;
D O I
10.3390/ijms23084181
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dysregulation of one-carbon metabolism affects a wide range of biological processes and is associated with a number of diseases, including cardiovascular disease, dementia, neural tube defects, and cancer. Accumulating evidence suggests that one-carbon metabolism plays an important role in COVID-19. The symptoms of long COVID-19 are similar to those presented by subjects suffering from vitamin B-12 deficiency (pernicious anemia). The metabolism of a cell infected by the SARS-CoV-2 virus is reshaped to fulfill the need for massive viral RNA synthesis, which requires de novo purine biosynthesis involving folate and one-carbon metabolism. Many aspects of host sulfur amino acid metabolism, particularly glutathione metabolism underlying antioxidant defenses, are also taken over by the SARS-CoV-2 virus. The purpose of this review is to summarize recent findings related to one-carbon metabolism and sulfur metabolites in COVID-19 and discuss how they inform strategies to combat the disease.
引用
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页数:15
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